Clinical Research Coordinator

Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH, GCP, protocol, and company guidelines, regulations, and policies. Ensures site receives accurate information and supplies from sponsors, educates potential participants and caregivers on protocol specific details and expectations, and performs safety and efficacy assessments per protocol.

Requirements

• High school graduate or equivalent; Bachelors Degree, preferred.
• 0-3 years of experience in the medical field.
• Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
• Strong leadership and mentorship skills.
• Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level.
• Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations.
• Works independently as well as functioning as part of a team.
• Must be able to effectively communicate verbally and in writing in English and Spanish.

Benefits

• Health Insurance
• Dental
• Vision
• LTD
• STD
• Life Ins
• 401k